Craniopharyngiomas are rare, partly cystic and calcified embryonic malformations of the
sellar/parasellar region with low histological grade (WHO Io). A bimodal age distribution has …

Hypothalamic syndrome (HS) is a rare disorder caused by disease-related and/or treatment-
related injury to the hypothalamus, most commonly associated with rare, non-cancerous …

Craniopharyngiomas (CPs) are clinically aggressive tumors because of their invasive
behavior and recalcitrant tendency to recur after therapy. There are 2 types based on their …

Craniopharyngioma (CP) is a rare embryonic malformation of the sellar/parasellar region
with a low histological grade. Clinical manifestations are related to hypothalamic/pituitary …

There is growing evidence that oxytocin (OXT), a hypothalamic hormone well recognized for
its effects in inducing parturition and lactation, has important metabolic effects in both sexes …

The hypothalamic peptide oxytocin and its receptor are involved in a range of physiological
processes, including parturition, lactation, cell growth, wound healing, and social behavior …

Background Disruptions of the hypothalamic–pituitary axis can cause an arginine
vasopressin deficiency, also known as central diabetes insipidus. Patients with this condition …

The development of hypothalamic obesity (HO) following craniopharyngioma (CP) and other
suprasellar tumors leads to reduced patient quality of life. No treatment algorithms are …

Childhood-onset craniopharyngiomas are rare embryonic tumours of low-grade histological
malignancy. Novel insights into the molecular pathogenesis of human adamantinomatous …

Craniopharyngiomas are rare embryonic malformational tumors of the sellar/parasellar
region, classified by the World Health Organization (WHO) as tumors with low-grade …